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富淋巴浆细胞脑膜瘤病例,类似肥厚性脑膜炎。

A case of Lymphoplasmacyte-rich meningioma mimicking pachymeningitis.

机构信息

Department of Neurology, Huashan Hospital, Fudan University, Shanghai, China.

Shanghai Medical College, Fudan University, Shanghai, China.

出版信息

BMC Neurol. 2022 Jul 29;22(1):283. doi: 10.1186/s12883-022-02794-z.

DOI:10.1186/s12883-022-02794-z
PMID:35906535
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9338539/
Abstract

BACKGROUND

Lymphoplasmacyte-rich meningioma (LPRM) is a rare form of meningioma characterized by prominent lymphoplasmacytic infiltrates into the tumor. Report of flat growth of LPRM mimicking pachymeningitis is rare in the literature.

CASE PRESENTATION

A 55-year-old female who suffered from episodes of headache and seizures has been diagnosed with pachymeningitis for 4 years because post contrast brain MRI demonstrated enhanced carpet-like dura lesion in the left frontal lobe. The lesion kept unchanged on yearly follow-ups until a recent brain MRI found the lesion grew significantly into a mass. The lesion was resected and pathology suggested LPRM.

CONCLUSION

LPRM may present as carpet-like growth pattern on MRI. Long-term follow-up in patients with pachymeningitis is necessary.

摘要

背景

淋巴浆细胞丰富型脑膜瘤(LPRM)是一种罕见的脑膜瘤,其特征是肿瘤内有明显的淋巴浆细胞浸润。文献中很少有报道 LPRM 呈扁平生长,类似于肥厚性脑膜炎。

病例介绍

一名 55 岁女性,反复发作头痛和癫痫,4 年来被诊断为肥厚性脑膜炎,因为增强脑 MRI 显示左额叶有增强的地毯样硬脑膜病变。该病变在每年的随访中保持不变,直到最近的脑 MRI 发现病变明显生长成一个肿块。该病变被切除,病理提示淋巴浆细胞丰富型脑膜瘤。

结论

LPRM 在 MRI 上可能表现为地毯样生长模式。肥厚性脑膜炎患者需要长期随访。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/680e/9338539/7ee28577411d/12883_2022_2794_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/680e/9338539/0fe11f971f7c/12883_2022_2794_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/680e/9338539/7ee28577411d/12883_2022_2794_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/680e/9338539/0fe11f971f7c/12883_2022_2794_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/680e/9338539/7ee28577411d/12883_2022_2794_Fig2_HTML.jpg

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